Simon White

发表

WGSA: an annotation pipeline for human genome sequencing studies

Andrew Carroll, Eric Boerwinkle, Bo Peng, 2015, Journal of Medical Genetics.

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.

G. Schellenberg, E. Wijsman, E. Boerwinkle, 2019, Genomics.

The population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequences.

R. Gibbs, Dahai Liu, D. Muzny, 2016, Genome research.

Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer’s Disease Sequencing Project

G. Schellenberg, E. Wijsman, E. Boerwinkle, 2018, bioRxiv.

The population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequences

R. Gibbs, Dahai Liu, D. Muzny, 2016, Genome research.

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline

R. Gibbs, E. Boerwinkle, D. Muzny, 2014, BMC Bioinformatics.

Assessing structural variation in a personal genome—towards a human reference diploid genome

Caleb F. Davis, P. Stankiewicz, J. Lupski, 2015, BMC Genomics.

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline

Simon White, Donna M. Muzny, Narayanan Veeraraghavan, 2014, BMC Bioinformatics.

A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease

Hiep D. Nguyen, J. Bressler, M. Fornage, 2018, Alzheimer's & Dementia.

Loss-of-function variants influence the human serum metabolome

Eric Boerwinkle, Alexander Hanbo Li, Richard A Gibbs, 2016, Science Advances.

Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel

Alexander Fedotov, Simon White, Eric Boerwinkle, 2018, Genetics in Medicine.

Assessing structural variation in a personal genome—towards a human reference diploid genome

Caleb F. Davis, P. Stankiewicz, J. Lupski, 2015, BMC Genomics.